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新型抗癌药物CKD-602的安全药理学

Safety pharmacology of CKD-602, a novel anticancer agent.

作者信息

Kim Eun Joo, Lee Rae Kyong, Suh Jeong Eun, Han Sang Seop, Kim Joon Kyum

机构信息

Toxicology Research Center, Korea Research Institute of Chemical Technology, Yuseong, Daejeon, Korea.

出版信息

Arzneimittelforschung. 2003;53(4):272-9. doi: 10.1055/s-0031-1297108.

Abstract

CKD-602 ((20S)-7-[2-(N-isopropylamino)-ethyl]-camptothecin.HCl, CAS 213819-48-8) is a new class of anticancer drug that belongs to the topoisomerase inhibitors. Its effect on the central nervous system (CNS), general behavior, cardiovascular-respiratory system and the other organ systems were studied. When intravenously administered, CKD-602 up to doses of 5 mg/kg caused an increase of body temperature, increase of respiration rate, decrease of gastrointestinal transport, showed analgesic action and produced antisecretory action in pylorus ligated rats. However, CKD-602 showed no effects on general behavior, motor coordination, spontaneous locomotor activity, hexobarbital sleeping time, convulsion, cardiovascular, smooth muscle and urinary tract system. These findings demonstrate that CKD-602 in doses up to 5 mg/kg has minor effects on the CNS in animals. However, CKD-602 does not exert any general pharmacological effects at the dose of 1 mg/kg except the effects on gastric secretion.

摘要

CKD - 602((20S)-7-[2-(N - 异丙基氨基)-乙基]-喜树碱盐酸盐,CAS 213819 - 48 - 8)是一类新型抗癌药物,属于拓扑异构酶抑制剂。研究了其对中枢神经系统(CNS)、一般行为、心血管呼吸系统及其他器官系统的影响。静脉注射时,高达5mg/kg剂量的CKD - 602可导致体温升高、呼吸频率增加、胃肠运输减慢,在幽门结扎大鼠中显示出镇痛作用并产生抗分泌作用。然而,CKD - 602对一般行为、运动协调性、自发运动活性、戊巴比妥睡眠时间、惊厥、心血管、平滑肌和泌尿系统均无影响。这些发现表明,高达5mg/kg剂量的CKD - 602对动物的中枢神经系统有轻微影响。然而,除了对胃分泌的影响外,1mg/kg剂量的CKD - 602不产生任何一般药理作用。

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